A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519031



Internal ID20892392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17816177..17817404hg38UCSC Ensembl
chr19:17926986..17928213hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381228
hg191228
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197708
Samples
Known GenesINSL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519031
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer